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Implications of Abscisic Acid in the Drought Stress Tolerance of Plants
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/jobm.201800309openalex-snapshot
Exopolysaccharides producing rhizobacteria and their role in plant growth and drought tolerance
inferredcites →https://doi.org/10.1006/bbrc.2000.4032openalex-snapshot
A Calmodulin Binding Protein from Arabidopsis Is Induced by Ethylene and Contains a DNA-Binding Motif
inferredcites →https://doi.org/10.1007/978-1-4614-7570-5_7openalex-snapshot
Drought Stress Signaling Network
inferredcites →https://doi.org/10.1007/978-3-030-30926-8_12openalex-snapshot
Growth and Yield of Field Crops Grown Under Drought Stress Condition Is Influenced by the Application of PGPR
inferredcites →https://doi.org/10.1007/978-3-319-99651-6_5openalex-snapshot
Role of PGPR in the Phytoremediation of Heavy Metals and Crop Growth Under Municipal Wastewater Irrigation
inferredcites →https://doi.org/10.1007/978-981-13-6536-2_4openalex-snapshot
Rhizobacteria and Abiotic Stress Management
inferredcites →https://doi.org/10.1007/s00425-010-1122-0openalex-snapshot
AtCPK6, a functionally redundant and positive regulator involved in salt/drought stress tolerance in Arabidopsis
inferredcites →https://doi.org/10.1007/s00425-010-1153-6openalex-snapshot
Calmodulin-binding transcription activator 1 mediates auxin signaling and responds to stresses in Arabidopsis
inferredcites →https://doi.org/10.1007/s00425-012-1745-4openalex-snapshot
Phospholipase Dδ is involved in nitric oxide-induced stomatal closure
inferredcites →https://doi.org/10.1007/s00438-011-0659-3openalex-snapshot
Comparative transcriptome analysis of AP2/EREBP gene family under normal and hormone treatments, and under two drought stresses in NILs setup by Aday Selection and IR64
inferredcites →https://doi.org/10.1007/s10265-008-0201-9openalex-snapshot
Activation of abscisic acid biosynthesis in the leaves of Arabidopsis thaliana in response to water deficit
inferredcites →https://doi.org/10.1007/s10265-015-0710-2openalex-snapshot
Identification of Arabidopsis thaliana NRT1/PTR FAMILY (NPF) proteins capable of transporting plant hormones
inferredcites →https://doi.org/10.1007/s10725-015-0034-1openalex-snapshot
The role of the CBL–CIPK calcium signalling network in regulating ion transport in response to abiotic stress
inferredcites →https://doi.org/10.1007/s10725-020-00571-xopenalex-snapshot
Crosstalk amongst phytohormones from planta and PGPR under biotic and abiotic stresses
inferredcites →https://doi.org/10.1007/s11103-016-0568-2openalex-snapshot
The protein phosphatase 2C clade A protein OsPP2C51 positively regulates seed germination by directly inactivating OsbZIP10
inferredcites →https://doi.org/10.1007/s11627-017-9874-xopenalex-snapshot
In vitro effects of GA3 on morphogenesis of CIP potato explants and acclimatization of plantlets in field
inferredcites →https://doi.org/10.1007/s11738-016-2335-zopenalex-snapshot
Chitosan alleviates phytotoxicity caused by boron through augmented polyamine metabolism and antioxidant activities and reduced boron concentration in Cucumis sativus L.
inferredcites →https://doi.org/10.1007/s12298-008-0008-0openalex-snapshot
Sucrose non-fermenting 1-related protein kinase 2 (SnRK2): a family of protein kinases involved in hyperosmotic stress signaling
inferredcites →https://doi.org/10.1007/s12374-013-0481-zopenalex-snapshot
Overexpressing a novel RING-H2 finger protein gene, OsRHP1, enhances drought and salt tolerance in rice (Oryza sativa L.)
inferredcites →https://doi.org/10.1007/s13199-016-0457-0openalex-snapshot
The root growth of wheat plants, the water conservation and fertility status of sandy soils influenced by plant growth promoting rhizobacteria
inferredcites →https://doi.org/10.1007/s13199-018-0583-yopenalex-snapshot
In vitro production of IAA by endophytic fungus Aspergillus awamori and its growth promoting activities in Zea mays
inferredcites →https://doi.org/10.1007/s13199-020-00690-zopenalex-snapshot
Yucasin and cinnamic acid inhibit IAA and flavonoids biosynthesis minimizing interaction between maize and endophyte Aspergillus nomius
inferredcites →https://doi.org/10.1016/0014-5793(92)81176-mopenalex-snapshot
A slow anion channel in guard cells, activating at large hyperpolarization, may be principal for stomatal closing
inferredcites →https://doi.org/10.1016/j.ab.2018.05.011openalex-snapshot
Assay for abscisic acid 8′-hydroxylase activity of cloned plant cytochrome P450 oxidases in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1016/j.agwat.2018.01.028openalex-snapshot
Drought stress in sunflower: Physiological effects and its management through breeding and agronomic alternatives
inferredcites →https://doi.org/10.1016/j.cell.2006.06.011openalex-snapshot
A Protein Kinase, Interacting with Two Calcineurin B-like Proteins, Regulates K+ Transporter AKT1 in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cell.2015.12.021openalex-snapshot
Adaptation of Root Function by Nutrient-Induced Plasticity of Endodermal Differentiation
inferredcites →https://doi.org/10.1016/j.cell.2016.08.029openalex-snapshot
Abiotic Stress Signaling and Responses in Plants
inferredcites →https://doi.org/10.1016/j.ecoenv.2019.05.037openalex-snapshot
Selenium impedes cadmium and arsenic toxicity in potato by modulating carbohydrate and nitrogen metabolism
inferredcites →https://doi.org/10.1016/j.envexpbot.2018.09.015openalex-snapshot
Polyamines provide new insights into the biochemical basis of Cr-tolerance in Kinnow mandarin grafted on diploid and double-diploid rootstocks
inferredcites →https://doi.org/10.1016/j.febslet.2007.07.051openalex-snapshot
CAMTAs: Calmodulin‐binding transcription activators from plants to human
inferredcites →https://doi.org/10.1016/j.febslet.2012.05.013openalex-snapshot
A plant microRNA regulates the adaptation of roots to drought stress
inferredcites →https://doi.org/10.1016/j.gene.2005.08.009openalex-snapshot
Molecular evolution of the AP2 subfamily
inferredcites →https://doi.org/10.1016/j.molcel.2011.05.011openalex-snapshot
The Molecular Basis of ABA-Independent Inhibition of PP2Cs by a Subclass of PYL Proteins
inferredcites →https://doi.org/10.1016/j.molp.2015.08.010openalex-snapshot
Two Faces of One Seed: Hormonal Regulation of Dormancy and Germination
inferredcites →https://doi.org/10.1016/j.molp.2016.11.011openalex-snapshot
Arabidopsis thaliana RECEPTOR DEAD KINASE1 Functions as a Positive Regulator in Plant Responses to ABA
inferredcites →https://doi.org/10.1016/j.molp.2018.06.009openalex-snapshot
The Flowering Repressor SVP Confers Drought Resistance in Arabidopsis by Regulating Abscisic Acid Catabolism
inferredcites →https://doi.org/10.1016/j.niox.2018.09.002openalex-snapshot
Abscisic acid and nitric oxide modulate cytoskeleton organization, root hair growth and ectopic hair formation in Arabidopsis
inferredcites →https://doi.org/10.1016/j.phytochem.2004.04.033openalex-snapshot
Proteomics of calcium-signaling components in plants
inferredcites →https://doi.org/10.1016/j.plantsci.2016.07.017openalex-snapshot
ABA accumulation in water-stressed Citrus roots does not rely on carotenoid content in this organ
inferredcites →https://doi.org/10.1016/j.plaphy.2013.07.004openalex-snapshot
A maize calcium-dependent protein kinase gene, ZmCPK4, positively regulated abscisic acid signaling and enhanced drought stress tolerance in transgenic Arabidopsis
inferredcites →https://doi.org/10.1016/j.plaphy.2018.02.013openalex-snapshot
The Arabidopsis GORK K+-channel is phosphorylated by calcium-dependent protein kinase 21 (CPK21), which in turn is activated by 14-3-3 proteins
inferredcites →https://doi.org/10.1016/j.scienta.2019.02.028openalex-snapshot
Rootstocks influence the salt tolerance of Kinnow mandarin trees by altering the antioxidant defense system, osmolyte concentration, and toxic ion accumulation
inferredcites →https://doi.org/10.1016/j.tplants.2008.10.005openalex-snapshot
The CBL–CIPK network in plant calcium signaling
inferredcites →https://doi.org/10.1016/j.tplants.2012.08.008openalex-snapshot
CDPKs in immune and stress signaling
inferredcites →https://doi.org/10.1016/j.ydbio.2006.12.037openalex-snapshot
Abscisic acid rescues the root meristem defects of the Medicago truncatula latd mutant
inferredcites →https://doi.org/10.1016/s0014-5793(01)03239-2openalex-snapshot
Calmodulin signaling via the IQ motif
inferredcites →https://doi.org/10.1021/jacs.8b08925openalex-snapshot
Unveiling Biosynthesis of the Phytohormone Abscisic Acid in Fungi: Unprecedented Mechanism of Core Scaffold Formation Catalyzed by an Unusual Sesquiterpene Synthase
inferredcites →https://doi.org/10.1023/a:1009253808876openalex-snapshot
Structures of EF-hand Ca 2+-binding proteins: Diversity in the organization, packing and response to Ca 2+ Binding
inferredcites →https://doi.org/10.1038/338427a0openalex-snapshot
Cytosolic calcium regulates ion channels in the plasma membrane of Vicia faba guard cells
inferredcites →https://doi.org/10.1038/346769a0openalex-snapshot
Elevation of cytoplasmic calcium by caged calcium or caged inositol trisphosphate initiates stomatal closure
inferredcites →https://doi.org/10.1038/35021067openalex-snapshot
Calcium channels activated by hydrogen peroxide mediate abscisic acid signalling in guard cells
inferredcites →https://doi.org/10.1038/35066500openalex-snapshot
Guard cell abscisic acid signalling and engineering drought hardiness in plants
inferredcites →https://doi.org/10.1038/nature06206openalex-snapshot
PLETHORA proteins as dose-dependent master regulators of Arabidopsis root development
inferredcites →https://doi.org/10.1038/nature07612openalex-snapshot
Ca2+/calmodulin regulates salicylic-acid-mediated plant immunity
inferredcites →https://doi.org/10.1038/nature08599openalex-snapshot
In vitro reconstitution of an abscisic acid signalling pathway
inferredcites →https://doi.org/10.1038/nature08794openalex-snapshot
Differential innate immune signalling via Ca2+ sensor protein kinases
inferredcites →https://doi.org/10.1038/nature09487openalex-snapshot
Homologue structure of the SLAC1 anion channel for closing stomata in leaves
inferredcites →https://doi.org/10.1038/nature10427openalex-snapshot
S-nitrosylation of NADPH oxidase regulates cell death in plant immunity
inferredcites →https://doi.org/10.1038/nature13663openalex-snapshot
PLETHORA gradient formation mechanism separates auxin responses
inferredcites →https://doi.org/10.1038/nchembio.1660openalex-snapshot
Rice cytochrome P450 MAX1 homologs catalyze distinct steps in strigolactone biosynthesis
inferredcites →https://doi.org/10.1038/ncomms11486openalex-snapshot
The Arabidopsis NPF3 protein is a GA transporter
inferredcites →https://doi.org/10.1038/ncomms9113openalex-snapshot
Abscisic acid transporters cooperate to control seed germination
inferredcites →https://doi.org/10.1038/nmeth.1769openalex-snapshot
Global profiling of dynamic protein palmitoylation
inferredcites →https://doi.org/10.1038/nsmb836openalex-snapshot
The ATP switch model for ABC transporters
inferredcites →https://doi.org/10.1038/s41586-018-0009-2openalex-snapshot
A small peptide modulates stomatal control via abscisic acid in long-distance signalling
inferredcites →https://doi.org/10.1038/s41598-018-36385-1openalex-snapshot
TaCAMTA4, a Calmodulin-Interacting Protein, Involved in Defense Response of Wheat to Puccinia triticina
inferredcites →https://doi.org/10.1038/s41598-019-38702-8openalex-snapshot
Comparative Physiological and Metabolic Analysis Reveals a Complex Mechanism Involved in Drought Tolerance in Chickpea (Cicer arietinum L.) Induced by PGPR and PGRs
inferredcites →https://doi.org/10.1038/sj.emboj.7600121openalex-snapshot
The Arabidopsis cytochrome P450 CYP707A encodes ABA 8′‐hydroxylases: key enzymes in ABA catabolism
inferredcites →https://doi.org/10.1038/srep27177openalex-snapshot
The ABA receptor PYL9 together with PYL8 plays an important role in regulating lateral root growth
inferredcites →https://doi.org/10.1038/srep31645openalex-snapshot
A calcium sensor – protein kinase signaling module diversified in plants and is retained in all lineages of Bikonta species
inferredcites →https://doi.org/10.1038/srep31772openalex-snapshot
Overexpression of calmodulin-like (ShCML44) stress-responsive gene from Solanum habrochaites enhances tolerance to multiple abiotic stresses
inferredcites →https://doi.org/10.1042/bj20091147openalex-snapshot
Breaking the code: Ca2+ sensors in plant signalling
inferredcites →https://doi.org/10.1042/bse0580029openalex-snapshot
Abscisic acid: biosynthesis, inactivation, homoeostasis and signalling
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00386.xopenalex-snapshot
Characterization of the ABA‐deficient tomato mutant notabilis and its relationship with maize Vp14
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00483.xopenalex-snapshot
Ethylene‐regulated gene expression in tomato fruit: characterization of novel ethylene‐responsive and ripening‐related genes isolated by differential display
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01096.xopenalex-snapshot
Regulation of drought tolerance by gene manipulation of 9‐ cis ‐epoxycarotenoid dioxygenase, a key enzyme in abscisic acid biosynthesis in Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01652.xopenalex-snapshot
An abscisic acid‐sensitive checkpoint in lateral root development of Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01663.xopenalex-snapshot
A Mak‐like kinase is a repressor of GAMYB in barley aleurone
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01786.xopenalex-snapshot
Molecular characterization of the Arabidopsis 9 ‐cis epoxycarotenoid dioxygenase gene family
inferredcites →https://doi.org/10.1073/pnas.0402112101openalex-snapshot
Phospholipase Dα1-derived phosphatidic acid interacts with ABI1 phosphatase 2C and regulates abscisic acid signaling
inferredcites →https://doi.org/10.1073/pnas.0504437102openalex-snapshot
Vacuolar Na + /H + antiporter cation selectivity is regulated by calmodulin from within the vacuole in a Ca 2+ - and pH-dependent manner
inferredcites →https://doi.org/10.1073/pnas.051616698openalex-snapshot
KAT1 is not essential for stomatal opening
inferredcites →https://doi.org/10.1073/pnas.0707912104openalex-snapshot
A protein phosphorylation/dephosphorylation network regulates a plant potassium channel
inferredcites →https://doi.org/10.1073/pnas.0709732105openalex-snapshot
Plant adaptation to fluctuating environment and biomass production are strongly dependent on guard cell potassium channels
inferredcites →https://doi.org/10.1073/pnas.0909222107openalex-snapshot
PDR-type ABC transporter mediates cellular uptake of the phytohormone abscisic acid
inferredcites →https://doi.org/10.1073/pnas.0912021106openalex-snapshot
Activity of guard cell anion channel SLAC1 is controlled by drought-stress signaling kinase-phosphatase pair
inferredcites →https://doi.org/10.1073/pnas.0912030107openalex-snapshot
Guard cell anion channel SLAC1 is regulated by CDPK protein kinases with distinct Ca 2+ affinities
inferredcites →https://doi.org/10.1073/pnas.1112151108openalex-snapshot
Induction of 9- cis -epoxycarotenoid dioxygenase in Arabidopsis thaliana seeds enhances seed dormancy
inferredcites →https://doi.org/10.1073/pnas.1116590109openalex-snapshot
Reconstitution of abscisic acid activation of SLAC1 anion channel by CPK6 and OST1 kinases and branched ABI1 PP2C phosphatase action
inferredcites →https://doi.org/10.1073/pnas.1203567109openalex-snapshot
Identification of an abscisic acid transporter by functional screening using the receptor complex as a sensor
inferredcites →https://doi.org/10.1073/pnas.122224699openalex-snapshot
Regulation of SOS1, a plasma membrane Na + /H + exchanger in Arabidopsis thaliana , by SOS2 and SOS3
inferredcites →https://doi.org/10.1073/pnas.1423481112openalex-snapshot
Nitric oxide negatively regulates abscisic acid signaling in guard cells by S-nitrosylation of OST1
inferredcites →https://doi.org/10.1073/pnas.2034853100openalex-snapshot
A novel domain in the protein kinase SOS2 mediates interaction with the protein phosphatase 2C ABI2
inferredcites →https://doi.org/10.1073/pnas.220426197openalex-snapshot
The Arabidopsis aldehyde oxidase 3 ( AAO3 ) gene product catalyzes the final step in abscisic acid biosynthesis in leaves
inferredcites →https://doi.org/10.1073/pnas.87.23.9305openalex-snapshot
Repetitive increases in cytosolic Ca2+ of guard cells by abscisic acid activation of nonselective Ca2+ permeable channels.
inferredcites →https://doi.org/10.1073/pnas.92.21.9535openalex-snapshot
Strong regulation of slow anion channels and abscisic acid signaling in guard cells by phosphorylation and dephosphorylation events.
inferredcites →https://doi.org/10.1073/pnas.94.22.12235openalex-snapshot
Genetic control of abscisic acid biosynthesis in maize
inferredcites →https://doi.org/10.1073/pnas.95.26.15837openalex-snapshot
Abscisic acid-induced stomatal closure mediated by cyclic ADP-ribose
inferredcites →https://doi.org/10.1073/pnas.96.26.15354openalex-snapshot
The 9- cis -epoxycarotenoid cleavage reaction is the key regulatory step of abscisic acid biosynthesis in water-stressed bean
inferredcites →https://doi.org/10.1074/jbc.m200268200openalex-snapshot
A Novel Family of Calmodulin-binding Transcription Activators in Multicellular Organisms
inferredcites →https://doi.org/10.1074/jbc.m207941200openalex-snapshot
A Calmodulin-binding/CGCG Box DNA-binding Protein Family Involved in Multiple Signaling Pathways in Plants
inferredcites →https://doi.org/10.1074/jbc.m303630200openalex-snapshot
The Crystal Structure of the Novel Calcium-binding Protein AtCBL2 from Arabidopsis thaliana
inferredcites →https://doi.org/10.1074/jbc.m504616200openalex-snapshot
Isolation of a Calmodulin-binding Transcription Factor from Rice (Oryza sativa L.)
inferredcites →https://doi.org/10.1079/ssr2005218openalex-snapshot
Plant hormone interactions during seed dormancy release and germination
inferredcites →https://doi.org/10.1080/14620316.2018.1504631openalex-snapshot
Genome-wide identification of citrus CAMTA genes and their expression analysis under stress and hormone treatments
inferredcites →https://doi.org/10.1080/15226514.2015.1064352openalex-snapshot
Role of plant growth promoting rhizobacteria and Ag-nano particle in the bioremediation of heavy metals and maize growth under municipal wastewater irrigation
inferredcites →https://doi.org/10.1080/15226514.2016.1203287openalex-snapshot
Modulation of phytoremediation and plant growth by the treatment with PGPR, Ag nanoparticle and untreated municipal wastewater
inferredcites →https://doi.org/10.1080/15226514.2017.1381940openalex-snapshot
Effects of exogenously applied salicylic acid and putrescine alone and in combination with rhizobacteria on the phytoremediation of heavy metals and chickpea growth in sandy soil
inferredcites →https://doi.org/10.1080/15592324.2018.1500069openalex-snapshot
Mechanisms for Abscisic Acid Inhibition of Primary Root Growth
inferredcites →https://doi.org/10.1080/17429145.2018.1471527openalex-snapshot
Effects of exogenously applied plant growth regulators in combination with PGPR on the physiology and root growth of chickpea (Cicer arietinum) and their role in drought tolerance
inferredcites →https://doi.org/10.1080/17429145.2018.1542041openalex-snapshot
IAA and flavonoids modulates the association between maize roots and phytostimulant endophytic Aspergillus fumigatus greenish
inferredcites →https://doi.org/10.1093/aob/mcr252openalex-snapshot
Abscisic acid and CO2 signalling via calcium sensitivity priming in guard cells, new CDPK mutant phenotypes and a method for improved resolution of stomatal stimulus-response analyses
inferredcites →https://doi.org/10.1093/emboj/20.5.1051openalex-snapshot
The NAF domain defines a novel protein–protein interaction module conserved in Ca2+‐regulated kinases
inferredcites →https://doi.org/10.1093/emboj/cdg277openalex-snapshot
NADPH oxidase AtrbohD and AtrbohF genes function in ROS‐dependent ABA signaling in Arabidopsis
inferredcites →https://doi.org/10.1093/jexbot/51.346.937openalex-snapshot
Extracellular β‐glucosidase activity in barley involved in the hydrolysis of ABA glucose conjugate in leaves
inferredcites →https://doi.org/10.1093/jxb/ert228openalex-snapshot
AtrbohD and AtrbohF positively regulate abscisic acid-inhibited primary root growth by affecting Ca2+ signalling and auxin response of roots in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/ert485openalex-snapshot
Hormonal control of cell division and elongation along differentiation trajectories in roots
inferredcites →https://doi.org/10.1093/jxb/erw477openalex-snapshot
Seed dormancy cycling and the regulation of dormancy mechanisms to time germination in variable field environments
inferredcites →https://doi.org/10.1093/mp/ssn003openalex-snapshot
Calcineurin-B-Like Protein CBL9 Interacts with Target Kinase CIPK3 in the Regulation of ABA Response in Seed Germination
inferredcites →https://doi.org/10.1093/mp/ssq064openalex-snapshot
Calcium-Dependent Protein Kinase CPK21 Functions in Abiotic Stress Response in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/mp/sst009openalex-snapshot
The Calcineurin B-Like Calcium Sensors CBL1 and CBL9 Together with Their Interacting Protein Kinase CIPK26 Regulate the Arabidopsis NADPH Oxidase RBOHF
inferredcites →https://doi.org/10.1093/pcp/pcq156openalex-snapshot
Molecular Basis of the Core Regulatory Network in ABA Responses: Sensing, Signaling and Transport
inferredcites →https://doi.org/10.1093/pcp/pcr194openalex-snapshot
Disruption of the Arabidopsis thaliana Inward-Rectifier K+ Channel AKT1 Improves Plant Responses to Water Stress
inferredcites →https://doi.org/10.1093/pcp/pcv063openalex-snapshot
Regulation of the NADPH Oxidase RBOHD During Plant Immunity
inferredcites →https://doi.org/10.1093/pcp/pcw051openalex-snapshot
Highly Sprouting-Tolerant Wheat Grain Exhibits Extreme Dormancy and Cold Imbibition-Resistant Accumulation of Abscisic Acid
inferredcites →https://doi.org/10.1104/pp.102.017921openalex-snapshot
Elucidation of the Indirect Pathway of Abscisic Acid Biosynthesis by Mutants, Genes, and Enzymes
inferredcites →https://doi.org/10.1104/pp.103.030734openalex-snapshot
A New Abscisic Acid Catabolic Pathway
inferredcites →https://doi.org/10.1104/pp.105.069757openalex-snapshot
Arabidopsis Calcium-Dependent Protein Kinase AtCPK32 Interacts with ABF4, a Transcriptional Regulator of Abscisic Acid-Responsive Gene Expression, and Modulates Its Activity
inferredcites →https://doi.org/10.1104/pp.105.070128openalex-snapshot
ABA-Hypersensitive Germination3Encodes a Protein Phosphatase 2C (AtPP2CA) That Strongly Regulates Abscisic Acid Signaling during Germination among Arabidopsis Protein Phosphatase 2Cs
inferredcites →https://doi.org/10.1104/pp.106.079327openalex-snapshot
Identification of Features Regulating OST1 Kinase Activity and OST1 Function in Guard Cells
inferredcites →https://doi.org/10.1104/pp.106.084632openalex-snapshot
Identification of Drought Tolerance Determinants by Genetic Analysis of Root Response to Drought Stress and Abscisic Acid
inferredcites →https://doi.org/10.1104/pp.108.116632openalex-snapshot
Drought Induction of Arabidopsis 9-cis-Epoxycarotenoid Dioxygenase Occurs in Vascular Parenchyma Cells
inferredcites →https://doi.org/10.1104/pp.110.157545openalex-snapshot
Arabidopsis Calcium-Dependent Protein Kinase CPK10 Functions in Abscisic Acid- and Ca2+-Mediated Stomatal Regulation in Response to Drought Stress
inferredcites →https://doi.org/10.1104/pp.113.220608openalex-snapshot
PYR/RCAR Receptors Contribute to Ozone-, Reduced Air Humidity-, Darkness-, and CO2-Induced Stomatal Regulation
inferredcites →https://doi.org/10.1104/pp.114.235556openalex-snapshot
Intertissue Signal Transfer of Abscisic Acid from Vascular Cells to Guard Cells
inferredcites →https://doi.org/10.1104/pp.114.239210openalex-snapshot
Abscisic Acid Uridine Diphosphate Glucosyltransferases Play a Crucial Role in Abscisic Acid Homeostasis in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.123.2.553openalex-snapshot
A Stress-Inducible Gene for 9-cis-Epoxycarotenoid Dioxygenase Involved in Abscisic Acid Biosynthesis under Water Stress in Drought-Tolerant Cowpea
inferredcites →https://doi.org/10.1104/pp.124.1.343openalex-snapshot
Characterization of the 9-Cis-Epoxycarotenoid Dioxygenase Gene Family and the Regulation of Abscisic Acid Biosynthesis in Avocado
inferredcites →https://doi.org/10.1104/pp.16.00328openalex-snapshot
Reactive Oxygen Species in the Regulation of Stomatal Movements
inferredcites →https://doi.org/10.1104/pp.16.01784openalex-snapshot
Drought-Enhanced Xylem Sap Sulfate Closes Stomata by Affecting ALMT12 and Guard Cell ABA Synthesis
inferredcites →https://doi.org/10.1104/pp.16.01945openalex-snapshot
ABA Suppresses Root Hair Growth via the OBP4 Transcriptional Regulator
inferredcites →https://doi.org/10.1104/pp.19.00119openalex-snapshot
CALMODULIN-BINDING TRANSCRIPTION ACTIVATOR 6: A Key Regulator of Na + Homeostasis during Germination
inferredcites →https://doi.org/10.1104/pp.83.1.33openalex-snapshot
Effect on Root Growth of Endogenous and Applied IAA and ABA
inferredcites →https://doi.org/10.1105/tpc.006494openalex-snapshot
A Unique Short-Chain Dehydrogenase/Reductase in Arabidopsis Glucose Signaling and Abscisic Acid Biosynthesis and Functions
inferredcites →https://doi.org/10.1105/tpc.007906openalex-snapshot
Arabidopsis OST1 Protein Kinase Mediates the Regulation of Stomatal Aperture by Abscisic Acid and Acts Upstream of Reactive Oxygen Species Production
inferredcites →https://doi.org/10.1105/tpc.010210openalex-snapshot
Abscisic Acid Activation of Plasma Membrane Ca2+ Channels in Guard Cells Requires Cytosolic NAD(P)H and Is Differentially Disrupted Upstream and Downstream of Reactive Oxygen Species Production in abi1-1 and abi2-1 Protein Phosphatase 2C Mutants
inferredcites →https://doi.org/10.1105/tpc.107.050666openalex-snapshot
Two Calcium-Dependent Protein Kinases, CPK4 and CPK11, Regulate Abscisic Acid Signal Transduction inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.108.061515openalex-snapshot
The Gibberellic Acid Signaling Repressor RGL2 Inhibits Arabidopsis Seed Germination by Stimulating Abscisic Acid Synthesis and ABI5 Activity
inferredcites →https://doi.org/10.1105/tpc.112.095935openalex-snapshot
A Vacuolar β-Glucosidase Homolog That Possesses Glucose-Conjugated Abscisic Acid Hydrolyzing Activity Plays an Important Role in Osmotic Stress Responses in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.100107openalex-snapshot
A Plasma Membrane Receptor Kinase, GHR1, Mediates Abscisic Acid- and Hydrogen Peroxide-Regulated Stomatal Movement in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.107227openalex-snapshot
Endodermal ABA Signaling Promotes Lateral Root Quiescence during Salt Stress in Arabidopsis Seedlings
inferredcites →https://doi.org/10.1105/tpc.112.108191openalex-snapshot
ArabidopsisPaired Amphipathic Helix Proteins SNL1 and SNL2 Redundantly Regulate Primary Seed Dormancy via Abscisic Acid–Ethylene Antagonism Mediated by Histone Deacetylation
inferredcites →https://doi.org/10.1105/tpc.114.125849openalex-snapshot
A Single-Pore Residue Renders the Arabidopsis Root Anion Channel SLAH2 Highly Nitrate Selective
inferredcites →https://doi.org/10.1105/tpc.114.133090openalex-snapshot
The Roles of ROS and ABA in Systemic Acquired Acclimation
inferredcites →https://doi.org/10.1105/tpc.16.00865openalex-snapshot
CAMTA-Mediated Regulation of Salicylic Acid Immunity Pathway Genes in Arabidopsis Exposed to Low Temperature and Pathogen Infection
inferredcites →https://doi.org/10.1105/tpc.7.11.1879openalex-snapshot
Gibberellin-regulated expression of a myb gene in barley aleurone cells: evidence for Myb transactivation of a high-pI alpha-amylase gene promoter.
inferredcites →https://doi.org/10.1111/1462-2920.14258openalex-snapshot
Biosynthesis of abscisic acid in fungi: identification of a sesquiterpene cyclase as the key enzyme in Botrytis cinerea
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02615.xopenalex-snapshot
ABA‐induced NO generation and stomatal closure in Arabidopsis are dependent on H 2 O 2 synthesis
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02701.xopenalex-snapshot
Use of the glucosyltransferase UGT71B6 to disturb abscisic acid homeostasis in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02881.xopenalex-snapshot
Regulation of hormone metabolism in Arabidopsis seeds: phytochrome regulation of abscisic acid metabolism and abscisic acid regulation of gibberellin metabolism
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03094.xopenalex-snapshot
The Arabidopsis ABA‐deficient mutant aba4 demonstrates that the major route for stress‐induced ABA accumulation is via neoxanthin isomers
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03236.xopenalex-snapshot
Two calcineurin B‐like calcium sensors, interacting with protein kinase CIPK23, regulate leaf transpiration and root potassium uptake in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03956.xopenalex-snapshot
Plasma membrane‐associated proline‐rich extensin‐like receptor kinase 4, a novel regulator of Ca2+ signalling, is required for abscisic acid responses in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04280.xopenalex-snapshot
ABA overly-sensitive 5 (ABO5), encoding a pentatricopeptide repeat protein required for cis-splicing of mitochondrial nad2 intron 3, is involved in the abscisic acid response in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04367.xopenalex-snapshot
ABA promotes quiescence of the quiescent centre and suppresses stem cell differentiation in the Arabidopsis primary root meristem
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04641.xopenalex-snapshot
Arabidopsis mutants of AtABCG22 , an ABC transporter gene, increase water transpiration and drought susceptibility
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04670.xopenalex-snapshot
The ethylene response factor AtERF11 that is transcriptionally modulated by the bZIP transcription factor HY5 is a crucial repressor for ethylene biosynthesis in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04887.xopenalex-snapshot
Epoxycarotenoid cleavage by NCED5 fine‐tunes ABA accumulation and affects seed dormancy and drought tolerance with other NCED family members
inferredcites →https://doi.org/10.1111/j.1399-3054.1984.tb06343.xopenalex-snapshot
The isolation and characterization of abscisic acid‐insensitive mutants of Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/jac.12169openalex-snapshot
Drought Stress in Grain Legumes during Reproduction and Grain Filling
inferredcites →https://doi.org/10.1111/jipb.12506openalex-snapshot
ARF2 coordinates with PLETHORAs and PINs to orchestrate ABA‐mediated root meristem activity in Arabidopsis
inferredcites →https://doi.org/10.1111/mpp.12075openalex-snapshot
Overexpression of GmCaM4 in soybean enhances resistance to pathogens and tolerance to salt stress
inferredcites →https://doi.org/10.1111/nph.12004openalex-snapshot
Abscisic acid accumulation modulates auxin transport in the root tip to enhance proton secretion for maintaining root growth under moderate water stress
inferredcites →https://doi.org/10.1111/nph.12469openalex-snapshot
Open Stomata 1 ( OST 1) is limiting in abscisic acid responses of Arabidopsis guard cells
inferredcites →https://doi.org/10.1111/nph.12607openalex-snapshot
b HLH 122 is important for drought and osmotic stress resistance in A rabidopsis and in the repression of ABA catabolism
inferredcites →https://doi.org/10.1111/nph.13882openalex-snapshot
Abscisic acid regulates root growth under osmotic stress conditions via an interacting hormonal network with cytokinin, ethylene and auxin
inferredcites →https://doi.org/10.1111/nph.15053openalex-snapshot
N‐myristoylation and S‐acylation are common modifications of Ca2+‐regulated Arabidopsis kinases and are required for activation of the SLAC1 anion channel
inferredcites →https://doi.org/10.1111/pbi.12066openalex-snapshot
Expression of an A rabidopsis molybdenum cofactor sulphurase gene in soybean enhances drought tolerance and increases yield under field conditions
inferredcites →https://doi.org/10.1111/pce.13195openalex-snapshot
UPLC‐HRMS‐based untargeted metabolic profiling reveals changes in chickpea ( Cicer arietinum ) metabolome following long‐term drought stress
inferredcites →https://doi.org/10.1111/ppl.12786openalex-snapshot
Overexpression of TaCML20 , a calmodulin‐like gene, enhances water soluble carbohydrate accumulation and yield in wheat
inferredcites →https://doi.org/10.1111/tpj.12534openalex-snapshot
Abscisic acid inhibits root growth in Arabidopsis through ethylene biosynthesis
inferredcites →https://doi.org/10.1111/tpj.13118openalex-snapshot
The Arabidopsis DELAY OF GERMINATION 1 gene affects ABSCISIC ACID INSENSITIVE 5 ( ABI 5) expression and genetically interacts with ABI 3 during Arabidopsis seed development
inferredcites →https://doi.org/10.1111/tpj.13646openalex-snapshot
Interaction network of ABA receptors in grey poplar
inferredcites →https://doi.org/10.1126/science.1172408openalex-snapshot
Regulators of PP2C Phosphatase Activity Function as Abscisic Acid Sensors
inferredcites →https://doi.org/10.1126/science.1215106openalex-snapshot
Molecular Mimicry Regulates ABA Signaling by SnRK2 Kinases and PP2C Phosphatases
inferredcites →https://doi.org/10.1126/science.276.5320.1872openalex-snapshot
Specific Oxidative Cleavage of Carotenoids by VP14 of Maize
inferredcites →https://doi.org/10.1126/science.280.5371.1943openalex-snapshot
A Calcium Sensor Homolog Required for Plant Salt Tolerance
inferredcites →https://doi.org/10.1126/science.aag1550openalex-snapshot
A transcription factor hierarchy defines an environmental stress response network
inferredcites →https://doi.org/10.1126/scisignal.2005051openalex-snapshot
The ABA Receptor PYL8 Promotes Lateral Root Growth by Enhancing MYB77-Dependent Transcription of Auxin-Responsive Genes
inferredcites →https://doi.org/10.1126/scisignal.2005703openalex-snapshot
Site- and kinase-specific phosphorylation-mediated activation of SLAC1, a guard cell anion channel stimulated by abscisic acid
inferredcites →https://doi.org/10.1126/scisignal.aaa7981openalex-snapshot
Inactivation of PYR/PYL/RCAR ABA receptors by tyrosine nitration may enable rapid inhibition of ABA signaling by nitric oxide in plants
inferredcites →https://doi.org/10.1146/annurev-arplant-042809-112226openalex-snapshot
Guard Cell Signal Transduction Network: Advances in Understanding Abscisic Acid, CO2, and Ca2+Signaling
inferredcites →https://doi.org/10.1146/annurev-arplant-042811-105501openalex-snapshot
Control of Arabidopsis Root Development
inferredcites →https://doi.org/10.1146/annurev.arplant.53.091401.143329openalex-snapshot
S ALT AND D ROUGHT S TRESS S IGNAL T RANSDUCTION IN P LANTS
inferredcites →https://doi.org/10.1146/annurev.bi.58.070189.004511openalex-snapshot
CRYSTAL STRUCTURES OF THE HELIX-LOOP-HELIX CALCIUM-BINDING PROTEINS
inferredcites →https://doi.org/10.1186/1471-2164-14-216openalex-snapshot
CAMTA 1 regulates drought responses in Arabidopsis thaliana
inferredcites →https://doi.org/10.1186/1471-2164-14-317openalex-snapshot
A burst of ABC genes in the genome of the polyphagous spider mite Tetranychus urticae
inferredcites →https://doi.org/10.1186/1471-2164-15-211openalex-snapshot
Identification, expression and interaction analyses of calcium-dependent protein kinase (CPK) genes in canola (Brassica napusL.)
inferredcites →https://doi.org/10.1186/1471-2229-14-8openalex-snapshot
Identification and characterization of CBL and CIPK gene families in canola (Brassica napus L.)
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Salicylic Acid Increases Photosynthesis of Drought Grown Mustard Plants Effectively with Sufficient-N via Regulation of Ethylene, Abscisic Acid, and Nitrogen-Use Efficiency
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Transcription factors PHR1 and PHR1-like 1 regulate ABA-mediated inhibition of seed germination and stomatal opening in Arabidopsis
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Physiological and transcriptional changes in soybean as adaptive responses to the combined effects of soil alkalinity and drought
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Genome-wide analysis and expression pattern profiling of the DUF789 gene family in soybean (Glycine max L.)
inferred← citeshttps://doi.org/10.1016/j.scienta.2025.113980openalex-snapshot
Genome-wide identification and expression profiling of the NCED gene family in salt and drought stress response of honeysuckle (Lonicera japonica thunb.)
inferred← citeshttps://doi.org/10.1016/j.scienta.2026.115004openalex-snapshot
Effects of combined application of selenium and polyaspartic acid-based water-retaining agent on the growth, drought resistance, yield and quality of tomato under drought stress
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2022.155120openalex-snapshot
Assessing Environmental Thresholds in Relation to Plant Structure and Nutritional Value for Improved Maize Calendar Ensuring Food Security
inferred← citeshttps://doi.org/10.1016/j.stress.2025.101166openalex-snapshot
Polyploidy modulates the adaptation to water deficit in citrus scion/rootstock associations evaluated under controlled pot condition and relates to specific changes in root and leaf transcriptome
inferred← citeshttps://doi.org/10.1016/j.stress.2026.101327openalex-snapshot
Maize responses to drought and Fusarium verticillioides infection: Mechanisms, potential interactions and management perspectives
inferred← citeshttps://doi.org/10.1021/acs.jafc.6c05637openalex-snapshot
Coordination of Abscisic Acid and Ultraviolet-B Radiations Dissociates Yield and Seed Quality Trade-Offs in Highland Barley under Water Deficit Stress
inferred← citeshttps://doi.org/10.1038/s41467-026-72169-2openalex-snapshot
Conserved and divergent gene regulatory networks for crop drought resistance
inferred← citeshttps://doi.org/10.1071/fp23280openalex-snapshot
Investigating the effect of drought stress and methanol spraying on the influential genes in the Calvin cycle and photorespiration of rapeseed (Brassica napus)
inferred← citeshttps://doi.org/10.1071/fp25173openalex-snapshot
ABA-centric signaling networks for drought resilience in cereals: from transcriptional reprogramming to epigenetic memory
inferred← citeshttps://doi.org/10.1079/9781800626102.0015openalex-snapshot
Plant Drought Resilience Based on Epigenetic Regulation
inferred← citeshttps://doi.org/10.1079/9781800626911.0015openalex-snapshot
Metabolomics-assisted Breeding: A New Omics-integrated Avenue for Improved Stress Response in Plants
inferred← citeshttps://doi.org/10.1080/01904167.2026.2659231openalex-snapshot
Biostimulants in modern agriculture: a comprehensive review of microbial and non-microbial categories, mechanisms, and sustainability implications
inferred← citeshttps://doi.org/10.1080/03235408.2024.2368112openalex-snapshot
Unveiling arbuscular mycorrhizal fungi: the hidden heroes of soil to control the plant pathogens
inferred← citeshttps://doi.org/10.1093/jxb/erac133openalex-snapshot
Molecular and physiological responses to desiccation indicate the abscisic acid pathway is conserved in the peat moss, Sphagnum
inferred← citeshttps://doi.org/10.1093/jxb/erae237openalex-snapshot
ABSCISIC ACID INSENSITIVE 3 promotes auxin signalling by regulating SHY2 expression to control primary root growth in response to dehydration stress
inferred← citeshttps://doi.org/10.1093/jxb/eraf097openalex-snapshot
PgMYB96 enhances Physalis grisea high temperature tolerance by activating trithorax-like factor WD REPEAT CONTAINING5b
inferred← citeshttps://doi.org/10.1093/jxb/eraf263openalex-snapshot
Iron retention coupled with trade-offs in localized symbiotic effects confers tolerance to combined iron deficiency and drought in soybean
inferred← citeshttps://doi.org/10.1101/2021.08.10.455871openalex-snapshot
Crosstalk between Ethylene and ABA during changes in soil water content reveals a role of ACC in coffee anthesis regulation
inferred← citeshttps://doi.org/10.1111/jac.70053openalex-snapshot
The Role of Trehalose in Improving Drought Tolerance in Wheat
inferred← citeshttps://doi.org/10.1111/plb.70141openalex-snapshot
Heterologous expression of α‐AtCAH1 improves resistance to drought stress and increases tuber yield in potato ( Solanum tuberosum L.)
inferred← citeshttps://doi.org/10.1111/ppl.13702openalex-snapshot
Ion transporters and their regulatory signal transduction mechanisms for salinity tolerance in plants
inferred← citeshttps://doi.org/10.1111/ppl.14195openalex-snapshot
Unveiling terahertz wave stress effects and mechanisms in Pinellia ternata: Challenges, insights, and future directions
inferred← citeshttps://doi.org/10.1111/ppl.70199openalex-snapshot
Reassessing Drought Tolerance in Citrus Tetraploid Rootstocks: Myth or Reality?
inferred← citeshttps://doi.org/10.1111/ppl.70202openalex-snapshot
MhNF ‐ YA2 modulates drought tolerance by triggering MhHSP70 ‐3 expression in Malus hupehensis
inferred← citeshttps://doi.org/10.1111/ppl.70519openalex-snapshot
Transcriptomic Analysis Reveals the Key Role of Photosynthetic System Stability and Carotenoid Accumulation in Drought Tolerance in Maize
inferred← citeshttps://doi.org/10.1111/ppl.70525openalex-snapshot
Moisture Matters: How Water Shapes Pest Invasions and Disease Outbreaks?
inferred← citeshttps://doi.org/10.1111/ppl.70821openalex-snapshot
Regulatory Role of Ubiquitin‐Proteasome System in Plant Responses to Drought Stress
inferred← citeshttps://doi.org/10.1111/ppl.71088openalex-snapshot
Integrating Plant Physiology and Microbiome Engineering for Climate‐Resilient Crops: Bridging Knowledge Gaps in Multi‐Stress Tolerance
inferred← citeshttps://doi.org/10.1111/ppl.71106openalex-snapshot
Dissecting the Role of Serotonin in Drought Responses of Rocket Plants: From Serotonin Accumulation to Tryptophan– ABA Associations
inferred← citeshttps://doi.org/10.1134/s1021443723602987openalex-snapshot
Comparison of the Effect of Mycorrhiza Fungi, Humic Acid, and Putrescine Treatments on Lallemantia royleana under Drought Stress
inferred← citeshttps://doi.org/10.1134/s1021443726600182openalex-snapshot
Chloroplast-Centered Acclimation to Sequential Stress Superior Drought Tolerance in Licorice via ROS Attenuation and Enhanced Recovery Sink
inferred← citeshttps://doi.org/10.1155/2021/6677616openalex-snapshot
Uptake, Translocation, and Consequences of Nanomaterials on Plant Growth and Stress Adaptation
inferred← citeshttps://doi.org/10.1186/s12870-021-03248-3openalex-snapshot
OsANN4 modulates ROS production and mediates Ca2+ influx in response to ABA
inferred← citeshttps://doi.org/10.1186/s12870-023-04136-8openalex-snapshot
Overexpression of OsERF106MZ promotes parental root growth in rice seedlings by relieving the ABA-mediated inhibition of root growth under salinity stress conditions
inferred← citeshttps://doi.org/10.1186/s12870-023-04354-0openalex-snapshot
Molecular network of the oil palm root response to aluminum stress
inferred← citeshttps://doi.org/10.1186/s12870-023-04709-7openalex-snapshot
TaWRKY31, a novel WRKY transcription factor in wheat, participates in regulation of plant drought stress tolerance
inferred← citeshttps://doi.org/10.1186/s12870-024-05982-wopenalex-snapshot
Genome-wide identification, classification, and expression profiling of LAC gene family in sesame
inferred← citeshttps://doi.org/10.1186/s12870-025-06417-wopenalex-snapshot
Functional analysis of the StERF79 gene in response to drought stress in potato (Solanum tuberosum L.)
inferred← citeshttps://doi.org/10.1186/s12870-025-07217-yopenalex-snapshot
Comparative physiological and transcriptomic profiling suggests key pathways in oat drought tolerance
inferred← citeshttps://doi.org/10.1186/s12870-025-08091-4openalex-snapshot
Heterologous expression of MfWRKY40 enhanced drought resistance of alfalfa
inferred← citeshttps://doi.org/10.1186/s12870-026-09298-9openalex-snapshot
Genome-wide identification and expression profiling of the ERF subfamily in Polygala tenuifolia seedlings under drought stress
inferred← citeshttps://doi.org/10.13057/biodiv/d240112openalex-snapshot
Relationship analysis of FaPYR1 and FaCHS genes encoding fruit ripening of three species of strawberries (Fragaria spp.) fruit
inferred← citeshttps://doi.org/10.13080/z-a.2023.110.014openalex-snapshot
Abscisic acid-induced response of Triticum aestivum and T. spelta phytohormonal system to moderate soil drought
inferred← citeshttps://doi.org/10.14500/aro.11033openalex-snapshot
Some Enzymatic and Non-enzymatic Antioxidants Response under Nickel and Lead Stress for Some Fabaceae Trees
inferred← citeshttps://doi.org/10.1590/1677-941x-abb-2023-0217openalex-snapshot
Influence of exogenous abscisic acid on physiological responses of Dendrobium candidum under drought stress
inferred← citeshttps://doi.org/10.17221/25/2023-ppsopenalex-snapshot
Exploring the role of endophytic fungi in the amelioration of drought stress in plants
inferred← citeshttps://doi.org/10.17221/628/2020-pseopenalex-snapshot
Effects of hydrogen peroxide application on agronomic traits of rice (Oryza sativa L.) under drought stress
inferred← citeshttps://doi.org/10.17521/cjpe.2022.0173openalex-snapshot
Sexual divergence of Populus deltoides seedlings growth and ecophysiological response to drought and rewatering
inferred← citeshttps://doi.org/10.17756/jfcn.2023-s1-048openalex-snapshot
Physiological and Biochemical Responses of Fruit Crops Under Stress
inferred← citeshttps://doi.org/10.21203/rs.3.rs-672361/v1openalex-snapshot
Salicylic Acid Increases Photosynthesis of Drought Grown Mustard Plants Effectively with Sufficient-N via Regulation of Ethylene, ABA and Nitrogen-Use Efficiency
inferred← citeshttps://doi.org/10.21608/ejbo.2022.150436.2045openalex-snapshot
The Physiological Response of Some Cotton Cultivars to Water Stress and Growth Inducers
inferred← citeshttps://doi.org/10.32604/phyton.2023.028317openalex-snapshot
An in Vitro Approach to Investigate the Role of Abscisic Acid in Alleviating the Negative Effects of Chilling Stress on Banana Shoots
inferred← citeshttps://doi.org/10.3389/fpls.2021.640443openalex-snapshot
Overexpression of the HDA15 Gene Confers Resistance to Salt Stress by the Induction of NCED3, an ABA Biosynthesis Enzyme
inferred← citeshttps://doi.org/10.3389/fpls.2022.1003907openalex-snapshot
Transcriptome profiling shows a rapid variety-specific response in two Andigenum potato varieties under drought stress
inferred← citeshttps://doi.org/10.3389/fpls.2022.1015317openalex-snapshot
Grafting enhances plants drought resistance: Current understanding, mechanisms, and future perspectives
inferred← citeshttps://doi.org/10.3389/fpls.2022.818472openalex-snapshot
Transcriptome Meta-Analysis Associated Targeting Hub Genes and Pathways of Drought and Salt Stress Responses in Cotton (Gossypium hirsutum): A Network Biology Approach
inferred← citeshttps://doi.org/10.3389/fpls.2022.824948openalex-snapshot
Crosstalk Between Ethylene and Abscisic Acid During Changes in Soil Water Content Reveals a New Role for 1-Aminocyclopropane-1- Carboxylate in Coffee Anthesis Regulation
inferred← citeshttps://doi.org/10.3389/fpls.2022.982622openalex-snapshot
Mild and severe salt stress responses are age-dependently regulated by abscisic acid in tomato
inferred← citeshttps://doi.org/10.3389/fpls.2023.1070302openalex-snapshot
Combining ability and testcross performance of multi-nutrient maize under stress and non-stress environments
inferred← citeshttps://doi.org/10.3389/fpls.2023.1167376openalex-snapshot
A holistic and sustainable approach linked to drought tolerance of Mediterranean crops
inferred← citeshttps://doi.org/10.3389/fpls.2023.1220928openalex-snapshot
Response of the organellar and nuclear (post)transcriptomes of Arabidopsis to drought
inferred← citeshttps://doi.org/10.3389/fpls.2023.1232583openalex-snapshot
Drought responsiveness in six wheat genotypes: identification of stress resistance indicators
inferred← citeshttps://doi.org/10.3389/fpls.2025.1713721openalex-snapshot
Melatonin mitigates cadmium-induced oxidative damage and modulates polysaccharide biosynthesis in Bletilla striata
inferred← citeshttps://doi.org/10.3390/agriculture11040285openalex-snapshot
Ameliorative Effects of Calcium Sprays on Yield and Grain Nutritional Composition of Maize (Zea mays L.) Cultivars under Drought Stress
inferred← citeshttps://doi.org/10.3390/agrochemicals2020019openalex-snapshot
Nanofertilizers: Types, Delivery and Advantages in Agricultural Sustainability
inferred← citeshttps://doi.org/10.3390/agrochemicals5010014openalex-snapshot
Environmental Impacts of Plant Growth Regulators in Modern Agriculture: Advances, Risks, and Sustainable Perspectives
inferred← citeshttps://doi.org/10.3390/agronomy10111683openalex-snapshot
Water Conservation and Plant Survival Strategies of Rhizobacteria under Drought Stress
inferred← citeshttps://doi.org/10.3390/agronomy11030524openalex-snapshot
Application of Plant Growth Promoting Microorganism and Plant Growth Regulators in Agricultural Production and Research
inferred← citeshttps://doi.org/10.3390/agronomy12010153openalex-snapshot
Towards Better Grafting: SCoT and CDDP Analyses for Prediction of the Tomato Rootstocks Performance under Drought Stress
inferred← citeshttps://doi.org/10.3390/agronomy12040813openalex-snapshot
Melatonin-Induced Resilience Strategies against the Damaging Impacts of Drought Stress in Rice
inferred← citeshttps://doi.org/10.3390/agronomy12102248openalex-snapshot
Chickpeas’ Tolerance of Drought and Heat: Current Knowledge and Next Steps
inferred← citeshttps://doi.org/10.3390/agronomy13030873openalex-snapshot
Endophytic Fusarium proliferatum Reprogrammed Phytohormone Production and Antioxidant System of Oryza sativa under Drought Stress
inferred← citeshttps://doi.org/10.3390/agronomy13082105openalex-snapshot
Stress Memories for Better Tolerance in Plants—A Potential Strategy for Crop Breeding
inferred← citeshttps://doi.org/10.3390/agronomy15102265openalex-snapshot
Integrated Approach of Using Biostimulants for Improving Growth, Physiological Traits, and Tolerance to Abiotic Stressors in Rice and Soybean
inferred← citeshttps://doi.org/10.3390/agronomy15102351openalex-snapshot
Irrigation Frequency Strategies and Deep Fertilization in Potato Crop
inferred← citeshttps://doi.org/10.3390/agronomy16030337openalex-snapshot
Physiological and Transcriptomic Responses of Asterothamnus centraliasiaticus Leaves to Drought Stress
inferred← citeshttps://doi.org/10.3390/biology13030194openalex-snapshot
The Response of Endogenous ABA and Soluble Sugars of Platycladus orientalis to Drought and Post-Drought Rehydration
inferred← citeshttps://doi.org/10.3390/biology14080965openalex-snapshot
Coordinated Regulation of Photosynthesis, Stomatal Traits, and Hormonal Dynamics in Camellia oleifera During Drought and Rehydration
inferred← citeshttps://doi.org/10.3390/biom11081159openalex-snapshot
Transcription Factors Interact with ABA through Gene Expression and Signaling Pathways to Mitigate Drought and Salinity Stress
inferred← citeshttps://doi.org/10.3390/bios14080378openalex-snapshot
Quantifying Plant Signaling Pathways by Integrating Luminescence-Based Biosensors and Mathematical Modeling
inferred← citeshttps://doi.org/10.3390/f15111967openalex-snapshot
Molecular Mechanisms of Poplar Adaptation to Water–Fertilizer Coupling: Insights from Transcriptomic and Metabolomic Analyses
inferred← citeshttps://doi.org/10.3390/f17020206openalex-snapshot
Molecular and Physiological Responses of Larix olgensis Seedlings to Drought and Exogenous ABA
inferred← citeshttps://doi.org/10.3390/genes15121529openalex-snapshot
Advances in Understanding Drought Stress Responses in Rice: Molecular Mechanisms of ABA Signaling and Breeding Prospects
inferred← citeshttps://doi.org/10.3390/horticulturae10080834openalex-snapshot
Molecular Responses to Drought and Waterlogging Stresses of Kiwifruit (Actinidia chinensis var. deliciosa) Potted Vines
inferred← citeshttps://doi.org/10.3390/horticulturae12050633openalex-snapshot
Chemotypic Diversity and Integrated Metabolic Profiling of Myrtle (Myrtus communis L.) from Mediterranean Turkey
inferred← citeshttps://doi.org/10.3390/horticulturae9020247openalex-snapshot
Comparative Analysis of Morphological, Physiological, Anatomic and Biochemical Responses in Relatively Sensitive Zinnia elegans ‘Zinnita Scarlet’ and Relatively Tolerant Zinnia marylandica ‘Double Zahara Fire Improved’ under Saline Conditions
inferred← citeshttps://doi.org/10.3390/ijms22115662openalex-snapshot
Plant Transcription Factors Involved in Drought and Associated Stresses
inferred← citeshttps://doi.org/10.3390/ijms23031084openalex-snapshot
Mechanisms of Abscisic Acid-Mediated Drought Stress Responses in Plants
inferred← citeshttps://doi.org/10.3390/ijms232416173openalex-snapshot
CRISPR/Cas9-Mediated Multiple Knockouts in Abscisic Acid Receptor Genes Reduced the Sensitivity to ABA during Soybean Seed Germination
inferred← citeshttps://doi.org/10.3390/ijms24065554openalex-snapshot
Metabolic Study of Cucumber Seeds and Seedlings in the Light of the New, Controversial Trend of Preventive Use of Systemic Fungicides
inferred← citeshttps://doi.org/10.3390/ijms24087580openalex-snapshot
Effects of Drought and Flooding on Phytohormones and Abscisic Acid Gene Expression in Kiwifruit
inferred← citeshttps://doi.org/10.3390/ijms24119628openalex-snapshot
Pre-Treatment of Rice Plants with ABA Makes Them More Tolerant to Multiple Abiotic Stress
inferred← citeshttps://doi.org/10.3390/ijms252010954openalex-snapshot
Stress-Responsive Gene Expression, Metabolic, Physiological, and Agronomic Responses by Consortium Nano-Silica with Trichoderma against Drought Stress in Bread Wheat
inferred← citeshttps://doi.org/10.3390/ijms26093944openalex-snapshot
The PAP Gene Family in Cotton: Impact of Genome-Wide Identification on Fiber Secondary Wall Synthesis
inferred← citeshttps://doi.org/10.3390/ijms26146986openalex-snapshot
The Identification of Transcriptomic and Phytohormonal Biomarkers for Monitoring Drought and Evaluating the Potential of Acibenzolar-S-Methyl Root Application to Prime Two Apple Rootstock Genotypes for Drought Resistance
inferred← citeshttps://doi.org/10.3390/plants10040796openalex-snapshot
Ameliorative Effects of Exogenous Proline on Photosynthetic Attributes, Nutrients Uptake, and Oxidative Stresses under Cadmium in Pigeon Pea (Cajanus cajan L.)
inferred← citeshttps://doi.org/10.3390/plants11131620openalex-snapshot
Plants’ Physio-Biochemical and Phyto-Hormonal Responses to Alleviate the Adverse Effects of Drought Stress: A Comprehensive Review
inferred← citeshttps://doi.org/10.3390/plants11223090openalex-snapshot
Recent Developments in the Application of Plant Growth-Promoting Drought Adaptive Rhizobacteria for Drought Mitigation
inferred← citeshttps://doi.org/10.3390/plants12091900openalex-snapshot
Proteomic Insights of Cowpea Response to Combined Biotic and Abiotic Stresses
inferred← citeshttps://doi.org/10.3390/plants13152111openalex-snapshot
Comparative Effects of Water Scarcity on the Growth and Development of Two Common Bean (Phaseolus vulgaris L.) Genotypes with Different Geographic Origin (Mesoamerica/Andean)
inferred← citeshttps://doi.org/10.3390/plants13192702openalex-snapshot
Biochemical and Proteomic Analyses in Drought-Tolerant Wheat Mutants Obtained by Gamma Irradiation
inferred← citeshttps://doi.org/10.3390/plants14111636openalex-snapshot
Physiological and Biochemical Adaptations to Repeated Drought–Rehydration Cycles in Ochroma lagopus Swartz: Implications for Growth and Stress Resilience
inferred← citeshttps://doi.org/10.3390/plants14121769openalex-snapshot
Physiologic, Genetic and Epigenetic Determinants of Water Deficit Tolerance in Fruit Trees
inferred← citeshttps://doi.org/10.3390/plants14172637openalex-snapshot
Annual Dynamics of Endogenous Hormones Reveal the Mechanism of Off-Season Flowering in Macadamia
inferred← citeshttps://doi.org/10.3390/plants15040640openalex-snapshot
Exogenous Abscisic Acid Enhances Water Use Efficiency and Drought Tolerance in Alfalfa (Medicago sativa L.)
inferred← citeshttps://doi.org/10.3390/plants15111700openalex-snapshot
Seed Hormonal Priming Improves Drought Resilience in Durum Wheat Through Modulation of Physiological and Biochemical Traits
inferred← citeshttps://doi.org/10.3390/plants15172653openalex-snapshot
Wheat Drought Management: A Broader Prospect
inferred← citeshttps://doi.org/10.3390/plants9101356openalex-snapshot
Identification, Evolutionary and Expression Analysis of PYL-PP2C-SnRK2s Gene Families in Soybean
inferred← citeshttps://doi.org/10.3390/proteomes14010004openalex-snapshot
Cross-Species Analysis of ABA-Induced Phosphosignaling Landscapes in Rice, Soybean, and Arabidopsis
inferred← citeshttps://doi.org/10.35537/10915/160121openalex-snapshot
Regulación fotoperiódica de la senescencia foliar post-floración en soja y en otras especies de importancia agronómica
inferred← citeshttps://doi.org/10.4018/979-8-3693-8648-4.ch018openalex-snapshot
Epigenetic Mechanisms Underlying Drought Tolerance in Plants
inferred← citeshttps://doi.org/10.46488/nept.2023.v22i04.039openalex-snapshot
Potassium Solubilizing Bacteria (KSB) and Osmopriming Mediated Morphological Changes and Triggers in Yield of Green Gram (Vigna radiata L.) Under Water-Limiting Conditions
inferred← citeshttps://doi.org/10.47328/ufvbbt.2022.423openalex-snapshot
Fertirrigação potássica por gotejamento no cultivo da batata
inferred← citeshttps://doi.org/10.48130/grares-0026-0006openalex-snapshot
ABA and MAPK signaling-mediated transcriptional regulation of drought and salinity responses in grasses
inferred← citeshttps://doi.org/10.52586/5021openalex-snapshot
An updated overview of the physiological and molecular responses of rice to anoxia
inferred← citeshttps://doi.org/10.56093/ijas.v91i4.112682openalex-snapshot
Stay-green trait ameliorates combined heat and drought stress in wheat
inferred← citeshttps://doi.org/10.56093/ijas.v93i8.138471openalex-snapshot
Unraveling the physiological and molecular mechanisms regulating grain yield under combined drought and heat stress in wheat (Triticum aestivum)
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